FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ARGYLE PEOCUSSOR SYSTEM

K Number: K771876 · Decision Oct 28, 1977
Classifications
1
FEI Numbers
35
Registration Numbers
35
Same Product Code
57
Applicant Total
62
Review Days
24

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Basic Information

Device Name
ARGYLE PEOCUSSOR SYSTEM
K Number
K771876
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5665
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Sherwood Medical Industries
Date Received
October 4, 1977
Decision Date
October 28, 1977
Product Code
BYI
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
BYI Percussor, Powered-Electric

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K792014 LANCER L-INA BUFFER, POLYMER, WASH SOLU
K782077 LANCER ICE CUBE
K790523 ARGYLE ESOPHAGEAL STETHOSCOPE
K790196 MONOJECT ARTERIAL BLOOD SAMPLING DEVICE
K790197 REAGENT KIT, LANCER GLUCOSE
K781459 MONOJECT SCALE MAGNIFIER
K781060 MONOJECT ENDOSSEOUS DENTAL IMPLANT
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